K-number	K082947
Device name	LENSX 550 LASER SYSTEM
Applicant	Lensx Lasers, Inc.
Product code	OOE
Device class	Class II
Decision date	Aug 14, 2009
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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LENSX 550 LASER SYSTEM

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